作者
Mitsuhide Naruse,Masanori Murakami,Takuyuki Katabami,Tomaž Kocjan,Mirko Parasiliti‐Caprino,Marcus Quinkler,Matthieu St‐Jean,Sam O’Toole,Filippo Ceccato,Ivana Kraljević,Darko Kaštelan,Mika Tsuiki,Jaap Deinum,Edelmiro Menéndez Torre,Troy Puar,Αthina Markou,George Piaditis,Kate Laycock,Norio Wada,Marianne Aardal Grytaas,Hiroki Kobayashi,Akiyo Tanabe,Chin Voon Tong,Nuria Valdés Gallego,Sven Gruber,Felix Beuschlein,Lydia Kürzinger,Norlela Sukor,Elena Azizan,Óskar Ragnarsson,Michiel F. Nijhoff,Giuseppe Maiolino,Guido Di Dalmazi,Valentina V. Kalugina,André Lacroix,Raluca Maria Furnica,Tomoko Suzuki
摘要
Abstract Objective Primary aldosteronism (PA) is one of the most frequent causes of secondary hypertension. Although clinical practice guidelines recommend a diagnostic process, details of the steps remain incompletely standardized. Design In the present SCOT-PA survey, we have investigated the diversity of approaches utilized for each diagnostic step in different expert centers through a survey using Google questionnaires. A total of 33 centers from 3 continents participated. Results We demonstrated a prominent diversity in the conditions of blood sampling, assay methods for aldosterone and renin, and the methods and diagnostic cutoff for screening and confirmatory tests. The most standard measures were modification of antihypertensive medication and sitting posture for blood sampling, measurement of plasma aldosterone concentration (PAC) and active renin concentration by chemiluminescence enzyme immunoassay, a combination of aldosterone-to-renin ratio with PAC as an index for screening, and saline infusion test in a seated position for confirmatory testing. The cutoff values for screening and confirmatory testing showed significant variation among centers. Conclusions Diversity of the diagnostic steps may lead to an inconsistent diagnosis of PA among centers and limit comparison of evidence for PA between different centers. We expect the impact of this diversity to be most prominent in patients with mild PA. The survey raises 2 issues: the need for standardization of the diagnostic process and revisiting the concept of mild PA. Further standardization of the diagnostic process/criteria will improve the quality of evidence and management of patients with PA.